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dc.contributor.advisorDalai, Dr.Ajay K.
dc.creatorKurhade, Ankeeta 1990-
dc.date.accessioned2019-12-16T19:40:50Z
dc.date.available2019-12-16T19:40:50Z
dc.date.created2019-11
dc.date.issued2019-12-16
dc.date.submittedNovember 2019
dc.identifier.urihttp://hdl.handle.net/10388/12487
dc.description.abstractBiodiesel, as a bioenergy source, is traditionally produced using alkaline catalysts which are limited to the use of refined vegetable oil feedstocks. The process tends to be environmentally non-benign because of undesired side reactions. It is important that this bioenergy is harnessed in a sustainable way. Heterogeneous solid acid catalysts can promote transesterification and esterification reactions from low-quality, unrefined feedstock without any side reactions like saponification or hydrolysis of triglycerides and minimize the effluent load downstream, thus, making them more desirable alternatives. The use of reactive and stable solid acid catalysts is one way of making the process sustainable. The primary aim of this research was to develop solid acid catalysts comprised of heteropolyacid like tungstophosphoric acid (HPW) and ordered mesoporous aluminosilicates such as MAS-7 and MAS-9. The work plan for this research was divided into five phases. In phase one, commercial γ-alumina was tested for the heterogenization of HPW. HPW loading of 45 wt % was found to be optimum giving a methyl ester yield of 90.0 ± 2.8 wt % for biodiesel synthesis from refined canola oil under optimized reaction conditions that is 10 wt % of the catalyst loading, 17.5 methanol to canola oil molar ratio, 4 MPa, and 200°C for 10 hr. In case of biodiesel production from unrefined green seed canola oil, the methyl ester yield observed was 74.0 ± 1.9 % at the above reaction conditions. Porous oxide material with acidic properties was determined to be suitable for heterogenization of HPW. However, complete disintegration of HPW at loadings of high concentrations (55 and 65 wt %) was observed on the γ-Al2O3 surface and hence, reduced the catalytic activity. Therefore, to tailor their properties mesoporous aluminosilicates such as MAS-7 and MAS-9 were used as supports in the next phase. The introduction of silica into the alumina framework has been shown to improve the textural and hydrothermal properties of alumina and hence in phase two, mesoporous aluminosilicates (MAS-7 and MAS-9) were selected as substitutes for γ-alumina as supports. A series of 5-45 wt % HPW on MAS-7/MAS-9 catalysts was prepared by a wet impregnation technique. Detailed insights into the surface chemistry of HPW supported on MAS catalysts were obtained with the help of Raman, Infrared, 29Si magic-angle spinning and cross-polarization/MAS nuclear magnetic resonance (NMR), and X-ray absorption spectroscopy. The catalytic activities were strongly correlated with the surface chemistry of the HPW supported on MAS-7 and MAS-9 catalysts. HPW supported on MAS-7 and MAS-9 exhibited favourable catalytic activity with a methyl ester yield of 76.5−88.7 wt % and stability sufficient for the simultaneous esterification and transesterification of low grade green seed canola oil. Based on this study, it was found that the MAS-7 and MAS-9 could serve as viable supports for the heterogenization of HPW. Therefore, the main goal in phase three was to enhance catalytic performance by tuning the textural characteristics of these materials. This was achieved by the direct incorporation of HPW into aluminosilicates resulting in HPW-MAS-7 and HPW-MAS-9 composites. These composites were obtained via a facile one-step assembly between positively charged ZSM-5 precursors and negatively charged PW12O403− species in the presence of the block copolymer. The textural characteristics of the composites were improved by introduction of HPW after the addition of an inorganic precursor to the template, leading to a material with a high BET surface area. Being novel heterogeneous solid acid catalysts, the activities of the composites were determined for biodiesel production from unrefined green seed canola oil, and yielded 95.4 ± 1.4 wt % of methyl esters in 10 h at 180 °C with 5.5 wt % of catalyst and a 15.5:1 methanol to oil molar ratio. Due to the high catalytic activity of these synthesized catalysts, it was decided to model the catalytic behaviour and investigate the techno-economic feasibility of scaling up this reaction for industrial application. In the fourth phase, kinetic modelling, mechanistic and thermodynamic studies were undertaken using an optimized HPW-MAS-9 catalyst. The experimental data were fitted to a pseudo-homogeneous model (PH) and adsorption-based models such as Eley-Rideal (ER) Langmuir–Hinshelwood-Hougen–Watson (LHHW). The activity coefficients of the reactant and product species were estimated using the UNIQUAC method. The Eley-Rideal reaction pathway with the surface reaction of adsorbed methanol as the rate controlling step, was found to be a reliable representation of the observed kinetics. In the fifth phase, techno-economic feasibility and life cycle analyses were conducted based on the results obtained in phase three. The economic analysis was performed using both deterministic and stochastic models. With the inclusion of tax incentives, the biodiesel selling price is approximately equal to $ 1.2 /kg and has a positive net present value (NPV) and an internal rate of return 25%. The results of these investigations revealed that the valorisation of green seed canola oil can be achieved by using HPW-MAS-9 catalyst; provided that there are appropriate incentives for the production of biodiesel. This research demonstrated that HPW-MAS-9 was not only an efficient heterogeneous catalyst for biodiesel synthesis, but also a material with tunable physicochemical properties that have potential relevance for industrial catalysis.
dc.format.mimetypeapplication/pdf
dc.subjectsolid acid catalysts
dc.subjecttransesterification
dc.titleSYNTHESIS AND CHARACTERIZATION OF SUPPORTED SOLID ACID CATALYSTS FOR CONVERSION OF GREEN SEED CANOLA OIL TO BIODIESEL
dc.typeThesis
dc.date.updated2019-12-16T19:40:51Z
thesis.degree.departmentChemical and Biological Engineering
thesis.degree.disciplineChemical Engineering
thesis.degree.grantorUniversity of Saskatchewan
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy (Ph.D.)
dc.type.materialtext
dc.contributor.committeeMemberSoltan, Dr.Jafar
dc.contributor.committeeMemberNiu, Dr.Catherine
dc.contributor.committeeMemberHu, Dr.Yongfeng
dc.contributor.committeeMemberTyler, Dr.Robert T.


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